@prefix this: <http://rdf.disgenet.org/nanopublications.trig#NP212201.RAeU8hkVpVYFeRVyxi2gs5cRtnlD8dl_C5QB2NXydltGQ> .
@prefix rdfs: <http://www.w3.org/2000/01/rdf-schema#> .
@prefix xsd: <http://www.w3.org/2001/XMLSchema#> .
@prefix sio: <http://semanticscience.org/resource/> .
@prefix ncit: <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#> .
@prefix lld: <http://linkedlifedata.com/resource/umls/id/> .
@prefix miriam-gene: <http://identifiers.org/ncbigene/> .
@prefix miriam-pubmed: <http://identifiers.org/pubmed/> .
@prefix eco: <http://purl.obolibrary.org/obo/eco.owl#> .
@prefix wi: <http://purl.org/ontology/wi/core#> .
@prefix prov: <http://www.w3.org/ns/prov#> .
@prefix pav: <http://purl.org/pav/2.0/> .
@prefix prv: <http://purl.org/net/provenance/ns#> .
@prefix dcterms: <http://purl.org/dc/terms/> .
@prefix np: <http://www.nanopub.org/nschema#> .
@prefix dgn-np: <http://rdf.disgenet.org/nanopublications.trig#> .
@prefix dgn-gda: <http://rdf.disgenet.org/gene-disease-association.ttl#> .
@prefix dgn-void: <http://rdf.disgenet.org/v2.1.0/void.ttl#> .

dgn-np:NP212201.RAeU8hkVpVYFeRVyxi2gs5cRtnlD8dl_C5QB2NXydltGQ130_head {
  this: np:hasAssertion dgn-np:NP212201.RAeU8hkVpVYFeRVyxi2gs5cRtnlD8dl_C5QB2NXydltGQ130_assertion;
    np:hasProvenance dgn-np:NP212201.RAeU8hkVpVYFeRVyxi2gs5cRtnlD8dl_C5QB2NXydltGQ130_provenance;
    np:hasPublicationInfo dgn-np:NP212201.RAeU8hkVpVYFeRVyxi2gs5cRtnlD8dl_C5QB2NXydltGQ130_publicationInfo;
    a np:Nanopublication .
  
  dgn-np:NP212201.RAeU8hkVpVYFeRVyxi2gs5cRtnlD8dl_C5QB2NXydltGQ130_assertion a np:Assertion .
  
  dgn-np:NP212201.RAeU8hkVpVYFeRVyxi2gs5cRtnlD8dl_C5QB2NXydltGQ130_provenance a np:Provenance .
  
  dgn-np:NP212201.RAeU8hkVpVYFeRVyxi2gs5cRtnlD8dl_C5QB2NXydltGQ130_publicationInfo a
      np:PublicationInfo .
}

dgn-np:NP212201.RAeU8hkVpVYFeRVyxi2gs5cRtnlD8dl_C5QB2NXydltGQ130_assertion {
  miriam-gene:1437 a ncit:C16612 .
  
  lld:C2939420 a ncit:C7057 .
  
  dgn-gda:DGNee20f9ebb0fa934306f4497c72582b61 sio:SIO_000628 miriam-gene:1437, lld:C2939420;
    a sio:SIO_001121 .
}

dgn-np:NP212201.RAeU8hkVpVYFeRVyxi2gs5cRtnlD8dl_C5QB2NXydltGQ130_provenance {
  dgn-np:NP212201.RAeU8hkVpVYFeRVyxi2gs5cRtnlD8dl_C5QB2NXydltGQ130_assertion dcterms:description
      "[Using microsatellite analysis, Southern blot analysis, and fluorescence in situ hybridization (FISH), 30 primary tumors and six CSF metastasis specimens were analyzed for loss of heterozygosity (LOH) of chromosomes 1q31, 6q, 9q22, 10q, 11, 16q22, and 17p13.1 and/or high-level amplification of the c-myc gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en;
    wi:evidence dgn-void:source_evidence_literature;
    sio:SIO_000772 miriam-pubmed:9667267;
    prov:wasDerivedFrom dgn-void:befree-20140225;
    prov:wasGeneratedBy eco:ECO_0000203 .
  
  dgn-void:befree-20140225 pav:importedOn "2014-02-25"^^xsd:date .
  
  dgn-void:source_evidence_literature a eco:ECO_0000212;
    rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en;
    rdfs:label "DisGeNET evidence - LITERATURE"@en .
}

dgn-np:NP212201.RAeU8hkVpVYFeRVyxi2gs5cRtnlD8dl_C5QB2NXydltGQ130_publicationInfo {
  this: dcterms:created "2014-10-02T12:33:57+02:00"^^xsd:dateTime;
    dcterms:rights <http://opendatacommons.org/licenses/odbl/1.0/>;
    dcterms:rightsHolder dgn-void:IBIGroup;
    dcterms:subject sio:SIO_000983;
    prv:usedData dgn-void:disgenetrdf;
    pav:authoredBy <http://orcid.org/0000-0001-5999-6269>, <http://orcid.org/0000-0002-7534-7661>,
      <http://orcid.org/0000-0002-9383-528X>, <http://orcid.org/0000-0003-0169-8159>, <http://orcid.org/0000-0003-1244-7654>;
    pav:createdBy <http://orcid.org/0000-0003-0169-8159>;
    pav:version "v2.1.0.0" .
  
  dgn-void:disgenetrdf pav:version "v2.1.0" .
}